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Saida Lahbib

2PUBLICATIONS

0CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)

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Publications (2)

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|May 18, 2019

Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family.

Saida Lahbib, Mediha Trabelsi, Hamza Dallali

|Oct 05, 2018

Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology.

Saida Lahbib, Claire S Leblond, Mariem Hamza

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